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15 Possible Causes for Mutation in the CALM2 Gene, Ventricular Tachycardia

  • Long QT Syndrome

    Here we present a girl 20 months of age with refractory ventricular tachycardia due to long QT syndrome successfully treated by left cardiac sympathetic denervation.[ncbi.nlm.nih.gov] RESULTS: A novel de novo CALM2 mutation (D132H) was discovered by candidate gene screening in a male infant with prenatal bradycardia born to healthy parents.[ncbi.nlm.nih.gov] LQTS indicates long-QT syndrome; CPVT, catecholaminergic polymorphic ventricular tachycardia.[doi.org]

  • Catecholaminergic Polymorphic Ventricular Tachycardia Type 2

    Abstract Objective Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a lethal inherited disease characterized by ventricular arrhythmias induced by physical[ncbi.nlm.nih.gov] […] that have been discovered and only represent a small percentage of CPVT cases are TRDN (encoding triadin) and CALM1 (encoding calmodulin). 5,6 Mutations in the CALM2 gene[doi.org] KCNJ2 mutations are associated with Andersen-Tawil syndrome and catecholaminergic polymorphic ventricular tachycardia.[ncbi.nlm.nih.gov]

  • Catecholaminergic Polymorphic Ventricular Tachycardia

    Treating Catecholaminergic Polymorphic Ventricular Tachycardia Symptoms Currently, there is no cure for Catecholaminergic Polymorphic Ventricular Tachycardia.[uwhealth.org] RYR2, CASQ2, KCNJ2 , ANK2, CALM1, CALM2, TRDN, SCN5A* Other Panels that Include this Diagnosis Notes on Genes: Priority Genes: These genes include 70% of the mutations that[admerahealth.com] […] induced by catecholamines Catecholamine-induced polymorphic ventricular tachycardia CPVT familial polymorphic ventricular tachycardia FPVT Cerrone M, Napolitano C, Priori[ghr.nlm.nih.gov]

  • Ventricular Arrhythmia

    Ventricular Tachycardia (VT) and Premature Ventricular Contractions (PVCs) This is a serious disorder and requires prompt treatment.[caifl.com] LQT15LQT15 is caused by heterozygous mutations in the CALM2 (Calmodulin 2) gene (114182) on chromosome 2p21.[en.wikipedia.org] What is ventricular tachycardia?[londonarrhythmiacentre.co.uk]

  • Long QT Syndrome 10

    I47.0 Re-entry ventricular arrhythmia I47.1 Supraventricular tachycardia I47.2 Ventricular tachycardia Reimbursement claims with a date of service on or after October 1,[icd10data.com] This prompted candidate-gene screening in a cohort of 82 LQTS genotype-negative patients. Two more patients were carriers of either CALM1 or CALM2 mutations.[smw.ch] Patients with this condition tend to develop severe arrhythmias such as ventricular tachycardia, especially polymorphic ventricular tachycardia (VT) or torsade de pointes[omicsonline.org]

  • Long QT Syndrome 13

    Monitor revealed a wide complex, polymorphic ventricular tachycardia, which reverted to sinus rhythm in a span of few seconds.[jtd.amegroups.com] This prompted candidate-gene screening in a cohort of 82 LQTS genotype-negative patients. Two more patients were carriers of either CALM1 or CALM2 mutations.[smw.ch] […] to Torsade de Pointes ventricular tachycardia.[ecgwaves.com]

  • Long QT Syndrome 15

    A successful electrical ablation of recurrent sustained ventricular tachycardia in a postoperative case of tetralogy of fallot.[med.niigata-u.ac.jp] Efficacy of procainamide and lidocaine in terminating sustained monomorphic ventricular tachycardia. Circ J. 2010;74:864-869 17.[med.niigata-u.ac.jp] Flecainide prevents catecholaminergic polymorphic ventricular tachycardia in mice and humans. Nature Medicine. 2009;15:380-383 22.[med.niigata-u.ac.jp]

  • Glycogen Storage Disease Type 9

    tachycardia Citrullinemia type II Combined oxidative phosphorylation defect type 4 Congenital fibrosis of extraocular muscles Congenital lactic acidosis, Saguenay-Lac-St.[csbg.cnb.csic.es] There are autosomal recessive forms of GSD IX (caused by mutations in PHKB, PHKG1, PHKG2, CALM1, CALM2, and CALM3 ), a X-linked liver form (caused by mutations in PHKA2 ),[bmcmedgenet.biomedcentral.com] tachycardia Laboratory Serum CK: Normal to 977 Cardiac enzymes: Mild elevation EMG: Myopathic EKG: Often normal Muscle MRI 36 Early involvement of deltoid & gluteus Legs:[neuromuscular.wustl.edu]

  • Glycogen Storage Disease due to Muscle Phosphorylase Kinase Deficiency

    tachycardia Citrullinemia type II Combined oxidative phosphorylation defect type 4 Congenital fibrosis of extraocular muscles Congenital lactic acidosis, Saguenay-Lac-St.[csbg.cnb.csic.es] There are autosomal recessive forms of GSD IX (caused by mutations in PHKB, PHKG1, PHKG2, CALM1, CALM2, and CALM3 ), a X-linked liver form (caused by mutations in PHKA2 ),[bmcmedgenet.biomedcentral.com] tachycardia Laboratory Serum CK: Normal to 977 Cardiac enzymes: Mild elevation EMG: Myopathic EKG: Often normal Muscle MRI 36 Early involvement of deltoid & gluteus Legs:[neuromuscular.wustl.edu]

  • Jervell-Lange-Nielsen Syndrome

    Keywords: Cervicothoracic sympathectomy, long QT syndrome, ventricular tachycardia How to cite this article: Roy PM, Khanna S, Mehta Y, Khan AZ.[ijaweb.org] A malignant form of LQTS associated to recurrent cardiac arrest due to VF in infants is associated to mutations in CALM1 and CALM2 genes encoding calmodulin (Crotti et al.[itaca.edu.es] Ventricular tachycardia with 2 variable opposing foci . Arch Mal Coeur Vaiss 1966 ; 59 : 263 – 272 . 10. Kleinman , CS , Glickstein , JS , Shaw , RF , et al .[cambridge.org]

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